Evaluation of a simple,inexpensive, in situ sampler for measuring time‐weighted average concentrations of suspended sediment in rivers and streams

The accurate measurement of suspended sediment (<200 μm) in aquatic environments is essential to understand and effectively manage changes to sediment, nutrient, and contaminant concentrations on both temporal and spatial scales. Commonly used sampling techniques for suspended sediment either lack the ability to accurately measure sediment concentration (e.g., passive sediment samplers) or are too expensive to deploy in sufficient number to provide landscape‐scale information (e.g., automated discrete samplers). Here, we evaluate a time‐integrated suspended sediment sampling technique, the pumped active suspended sediment (PASS) sampler, which collects a sample that can be used for the accurate measurement of time‐weighted average (TWA) suspended sediment concentration and sediment particle size distribution. The sampler was evaluated against an established passive time‐integrated suspended sediment sampling technique (i.e., Phillips sampler) and the standard discrete sampling method (i.e., manual discrete sampling). The PASS sampler collected a sample representative of TWA suspended sediment concentration and particle size distribution of a control sediment under laboratory conditions. Field application of the PASS sampler showed that it collected a representative TWA suspended sediment concentration and particle size distribution during high flow events in an urban stream. The particle size distribution of sediment collected by the PASS and Phillips samplers were comparable and the TWA suspended sediment concentration of the samples collected using the PASS and discrete sampling techniques agreed well, differing by only 4% and 6% for two different high flow events. We should note that the current configuration of the PASS sampler does not provide a flow‐weighted measurement and, therefore, is not suitable for the determination of sediment loads. The PASS sampler is a simple, inexpensive, and robust in situ sampling technique for the accurate measurement of TWA suspended sediment concentration and particle size distribution.     

Passive Samplers for Monitoring VOCs in Groundwater and the Prospects Related to Mass Flux Measurements

Measurement and interpretation of mass fluxes in favor of concentrations is gaining more and more interest, especially within the framework of the characterization and management of large-scale volatile organic carbon (VOC) groundwater contamination (source zones and plumes). Traditional methods of estimating contaminant fluxes and discharges involve individual measurements/calculations of the Darcy water flux and the contaminant concentrations. However, taken into account the spatially and temporally varying hydrologic conditions in complex, heterogeneous aquifers, higher uncertainty arises from such indirect estimation of contaminant fluxes. Therefore, the potential use of passive sampling devices for the direct measurement of groundwater-related VOC mass fluxes is examined. A review of current passive samplers for the measurement of organic contaminants in water yielded the selection of 18 samplers that were screened for a number of criteria. These criteria are related to the possible application of the sampler for the measurement of VOC mass fluxes in groundwater. This screening study indicates that direct measurement of VOC mass fluxes in groundwater is possible with very few passive samplers. Currently, the passive flux meter (PFM) is the only passive sampler which has proven to effectively measure mass fluxes in near source groundwater. A passive sampler for mass flux measurement in plume zones with regard to long-term monitoring (several months to a year) still needs to be developed or optimized. A passive sampler for long-term monitoring of contaminant mass fluxes in groundwater would be of considerable value in the development of risk-based assessment and management of soil and groundwater pollutions.     

A Portable Membrane Contactor Sampler for Analysis of Noble Gases in Groundwater

To enable a wider use of dissolved noble gas concentrations and isotope ratios in groundwater studies, we have developed an efficient and portable sampling device using a commercially available membrane contactor. The device separates dissolved gases from a stream of water and collects them in a small copper tube (6 mm in diameter and 100 mm in length with two pinch‐off clamps) for noble gas analysis by mass spectrometry. We have examined the performance of the sampler using a tank of homogeneous water prepared in the laboratory and by field testing. We find that our sampling device can extract heavier noble gases (Ar, Kr, and Xe) more efficiently than the lighter ones (He and Ne). An extraction time of about 60 min at a flow rate of 3 L/min is sufficient for all noble gases extracted in the sampler to attain equilibrium with the dissolved phase. The extracted gas sample did not indicate fractionation of helium (³He/⁴He) isotopes or other noble gas isotopes. Field performance of the sampling device was tested using a groundwater well in Vienna and results were in excellent agreement with those obtained from the conventional copper tube sampling method.     

Automated water sampling in ephemeral hydrological systems

A wide variety of sampling programmes may now be considered practical with the recent developments in data logger and water sampler technology. In ephemeral systems the water sampler remains idle for long periods between events. Two approaches are described which overcome the problems of sampling in ephemeral systems: short interval time dependent sampling (TDS) and automated flow proportional sampling (FPS). Both approaches utilize the data logger's ability to perform intermediate operations on incoming data to control the initiation of water sampling. The logger programs are described and allow many recorder/water sampler units to be controlled from one device. The relative merits of the two approaches are discussed in terms of experimental requirements and data precision.     

Evaluation of Passive Diffusive-Adsorptive Samplers for Use in Assessing Time-Varying Indoor Air Impacts Resulting from Vapor Intrusion

Passive diffusive-adsorptive samplers are being considered for vapor intrusion (VI) pathway assessment, particularly where multi-week time-weighted average concentrations are desired. Recent studies have shown that passive samplers can produce accurate results under well-controlled steady concentration conditions, and field performance was also demonstrated at several sites. The objective of this study was to examine passive sampler performance in settings with time-varying indoor air concentrations, through a comparison of passive sampler results to concentrations determined by 24-h active sorbent tube sampling in a series of multi-week deployments. Sampling was performed in a well-instrumented residential building as well as industrial buildings, over periods of time ranging from 1 to 7 weeks. Strong linear correlations were noted between passive and active sampling concentration results for some passive samplers, with passive sampling results being similar to or lower than measured active sampling results by about 50% for those samplers in the residential study and about 25% higher in the industrial building study. Other samplers produced poor agreement. The conclusion from this study is that some passive samplers have great potential for use in multi-week indoor air quality monitoring. It was further determined that there is need for accepted procedures to validate and calibrate passive samplers for use in the field.     

Measurements of free radicals in the atmosphere by matrix isolation and electron paramagnetic resonance

With some special adaptations the technique of matrix isolation followed by detection through electron paramagnetic resonance (EPR) can also be used for the measurement of atmospheric radical concentrations. A light weight cryogenic sampling device has been constructed. It uses condensation of atmospheric CO₂ or H₂O at 77 K for matrix formation and trapping of the radicals. The sampler has been flown on a balloon for stratospheric sampling. First data on stratospheric, HO₂ and NO₂ at 32 km altitude have been obtained on a flight on 8 August 1976 and will be reported.     

Event monitoring of herbicides with naked and membrane-covered Empore disk integrative passive sampling devices

Subsequent to an initial wet season flood event in the Brisbane River, Australia, both fast (naked disk) and slow (membrane-covered) variants of SDB-RPS Empore disk passive sampling devices were deployed with an automated grab sampling program. A trend increase in the aquatic dissolved concentrations of diuron and simazine was observed over a 10-day period. Kinetic and equilibrium parameters for each sampler were calculated based on the dynamic concentration. Absolute percent difference for duplicate passive samples was <10% in the fast and <25% in the slow samplers. For kinetic sampling, significantly shortened integrative periods are available with the fast compared with the slow variant, with higher sampling rates offering improved detection limits. The study demonstrates a method for determining kinetic parameters of passive samplers in a variable concentration field deployment, and illustrates the differences in quality between active and passive data, in terms of capturing changes in concentration associated with rainfall events.     

Concepts for measuring horizontal groundwater flow directions using the passive flux meter

The passive flux meter (PFM) is a permeable down-hole device designed to measure the magnitudes of horizontal groundwater specific discharge and contaminant mass flux in porous media. By means of a geometrical analysis of resident tracer transport inside a PFM, this paper introduces two new PFM designs capable of measuring both the direction and magnitude of horizontal water and contaminant fluxes. One design relies on the detection of a single resident tracer over multiple domains within the PFM cross section to determine the magnitude and direction of water flux. The second PFM configuration uses the detected loss of multiple resident tracers in different sectors of the PFM cross section to generate the same characterization of water flux. Both designs rely on the assumption of linear, instantaneous and reversible tracer sorption.     

A Proposed Method to Estimate In Situ Dissolved Gas Concentrations in Gas‐Saturated Groundwater

Gas‐saturated groundwater forms bubbles when brought to atmospheric pressure, preventing precise determination of its in situ dissolved gas concentrations. To overcome this problem, a modeling approach called the atmospheric sampling method is suggested here to recover the in situ dissolved gas concentrations of groundwater collected ex situ under atmospheric conditions at the Horonobe Underground Research Laboratory, Japan. The results from this method were compared with results measured at the same locations using two special techniques, the sealed sampler and pre‐evacuated vial methods, that have been developed to collect groundwater under its in situ conditions. In gas‐saturated groundwater cases, dissolved methane and inorganic carbon concentrations derived using the atmospheric sampling method were mostly within ±4 and ±10%, respectively, of values from the sealed sampler and pre‐evacuated vial methods. In gas‐unsaturated groundwater, however, the atmospheric sampling method overestimated the in situ dissolved methane concentrations, because the groundwater pressure at which bubbles appear (P_critical) was overestimated. The atmospheric sampling method is recommended for use where gas‐saturated groundwater can be collected only ex situ under atmospheric conditions.     

Laboratory calibration of chemical volcanic gas sampling techniques using an artificial fumarole

We have constructed an artificial laboratory fumarole to calibrate the most common chemical volcanic gas sampling techniques and obtain a quantitative measure of their efficacy. We have also developed and tested a new rugged and portable venturi spray gas sampler. The venturi sampler reproduced the output gas composition most accurately, followed by the Giggenbach bottles, filter packs, and lastly alkaline traps. Passive alkaline traps, however, did better than filter packs when sampling more concentrated fumarole gases. Under ideal conditions, the accuracy of the Giggenbach bottles was identical to the venturi sampler, although there was slightly more scatter. The Giggenbach sampler was more susceptible to problems with condensation on the input train even in a laboratory setting, and this technique was only effective in relatively concentrated gas streams. Filter packs are also effective, but extreme care must be exercised to maintain strong undersaturation with respect to the acid gas. If strong undersaturation (high pH) is not maintained, the filter packs return erroneously low S/Cl and S/F ratios. Use of a pH indicator is an effective way of avoiding this problem. The passive alkaline traps also under-sample sulfur, resulting in low reported S/Cl and S/F ratios. It appears that the overall sampling efficiency of all techniques was not strongly affected by oxygen fugacity over the limited range tested. When detecting sulfate and sulfite simultaneously, we found no difference in total sulfur before and after oxidation. This suggests that all sulfur from the gas regardless of oxidation state was absorbed as sulfite or sulfate and/or was quickly oxidized in solution. This conclusion is supported by IC HS⁻ reference samples.     

Groundwater Flow Field Distortion by Monitoring Wells and Passive Flux Meters

Due to differences in hydraulic conductivity and effects of well construction geometry, groundwater lateral flow through a monitoring well typically differs from groundwater flow in the surrounding aquifer. These differences must be well understood in order to apply passive measuring techniques, such as passive flux meters (PFMs) used for the measurement of groundwater and contaminant mass fluxes. To understand these differences, lab flow tank experiments were performed to evaluate the influences of the well screen, the surrounding filter pack and the presence of a PFM on the natural groundwater flux through a monitoring well. The results were compared with analytical calculations of flow field distortion based on the potential theory of Drost et al. (1968). Measured well flow field distortion factors were found to be lower than calculated flow field distortion factors, while measured PFM flow field distortion factors were comparable to the calculated ones. However, this latter is not the case for all conditions. The slotted geometry of the well screen seems to make a correct analytical calculation challenging for conditions where flow field deviation occurs, because the potential theory assumes a uniform flow field. Finally, plots of the functional relationships of the distortion of the flow field with the hydraulic conductivities of the filter screen, surrounding filter pack and corresponding radii make it possible to design well construction to optimally function during PFM applications.     

The Use of Industrial Hygiene Samplers for Soil-Gas Surveying

Soil-gas surveying by the use of a passive sampler which allows quantitative determination of concentrations of volatile organic compounds and remote analysis of samples is described. The results of a survey using the sampler above a chloroform ground water plume are compared to ground water analysis results and to results from a previous soil-gas study above the same plume. Chloroform concentrations measured with passive samplers correlate well (r = 0.79, n = 6; r = 0.93, n = 7) with the other two techniques. The short-range variability of the technique is characterized by a coefficiet of variation of 12 percent over a 27-foot distance for nine samplers, and compares favorably with grab-sample results at the same location.     

Continuous measurement of nitrate concentration in a highly event‐responsive agricultural catchment in south‐west of France: is the gain of information useful?

A nitrate sensor has been set up to measure every 10 min the nitrate signal in a stream draining a small agricultural catchment dominated by fertilized crops during a 2‐year study period (2006–2008) in the south‐west of France. An in situ sampling protocol using automatic sampler to monitor flood events have been used to assume a point‐to‐point calibration of the sensor values. The nitrate concentration exhibits nonsystematic concentration and dilution effects during flood events. We demonstrate that the calibrated nitrate sensor signal gathered from the outlet is considered to be a continuous signal using the Nyquist–Shannon sampling theorem. The objectives of this study are to quantify the errors generated by a typical infrequent sampling protocol and to design appropriate sampling strategy according to the sampling objectives. Nitrate concentration signal and flow data are numerically sampled to simulate common sampling frequencies. The total fluxes calculated from the simulated samples are compared with the reference value computed on the continuous signal. Uncertainties are increasing as sampling intervals increase; the method that is not using continuous discharge to compute nitrate fluxes bring larger uncertainty. The dispersion and bias computed for each sampling interval are used to evaluate the uncertainty during each hydrological period. High underestimation is made during flood periods when high‐concentration period is overlooked. On the contrary, high sampling frequencies (from 3 h to 1 day) lead to a systematic overestimation (bias around 3%): highest concentrations are overweighted by the interpolation of the concentration in such case. The in situ sampling protocol generates less than 1% of load estimation error and sample highest concentration peaks. We consider useful such newly emerging field technologies to assess short‐term variations of water quality parameters, to minimize the number of samples to be analysed and to assess the quality state of the stream at any time. Copyright © 2012 John Wiley & Sons, Ltd.     

Suspended sediment monitoring in alluvial gullies: A laboratory and field evaluation of available measurement techniques

Gully erosion is a significant source of fine suspended sediment (<63 μm) and associated nutrient pollution to freshwater and marine waterways. Researchers, government agencies, and monitoring groups are currently using monitoring methods designed for streams and rivers (e.g., autosamplers, rising stage samplers, and turbidity loggers) to evaluate suspended sediment in gullies. This is potentially problematic because gullies have several hydrological features and monitoring operational challenges that differ to those of continually flowing streams and rivers (e.g., short and intense flows, high suspended sediment concentrations, and rapid scouring and aggradation). Here we present a laboratory and field-based assessment of the performance of common suspended sediment monitoring techniques applied to gullies. We also evaluate a recently-described method; the pumped active suspended sediment (PASS) sampler, which has been modified for monitoring suspended sediment in gully systems. Discrete autosampling provided data at high temporal resolution, however, it had poor collection efficiency (25 ± 10%) of coarser sediment particles (i.e., sand). Rising stage sampling, while robust and cost-effective, suffered from large amounts of condensation under field conditions (25–35% of sampler volume), due to harsh climatic conditions creating large diurnal temperature differences at the field site, thereby diluting sample concentrations and introducing additional measurement uncertainty. The turbidity logger exhibited a highly variable response when calibrated at each site with physically collected suspended sediment samples (R² = 0.17–0.83), highlighting that this approach should be used with caution. The modified PASS sampler proved to be a reliable and representative measurement method for gully sediment water quality, however, the time-integrated nature of the method limits its temporal resolution compared to the other monitoring methods. We recommend monitoring suspended sediment in alluvial gully systems using a combination of complementary techniques (e.g., PASS and RS samplers) to account for the limitations associated with individual methods.     

Brown mussels (Perna perna) and semi-permeable membrane devices (SPMDs) as indicators of organic pollutants in the South African marine environment

A distinct lack of historical and current data on the status of organic pollutant contaminants within the South African marine environment is evident. This has highlighted the need for more current organic pollutant assessments. Reference mussels and SPMDs were transplanted at five South African harbour sites to assess organic bioaccumulation in brown mussels (Perna perna) and semi-permeable membrane devices (SPMDs). Spatial patterns of PAH and PCB contaminants were determined by GC-MS and GC-ECD after appropriate sample preparation. Significant (p<0.05) spatial differences were observed between the sites. Results indicate no correlations between the passive device and the transplanted mussels; however the SPMDs provided complementary information on the presence of dioxin-like PCBs within the environment not detected by the mussel. The results indicate that information provided by both the mussels and SPMDs allow for a more in depth scrutiny of environmental conditions as a result of anthropogenic influence.     

Preliminary evaluation of the occurrence of herbicides and PAHs in the Wet Tropics region of the Great Barrier Reef, Australia, using passive samplers

The proximity of the Great Barrier Reef (GBR) Marine Park to areas of intensive agriculture and increasing urbanisation places the park under potential threat of contamination by land-based pollutants. Passive samplers were deployed at inshore reef and river mouth sites in the Wet Tropics region of the GBR during a dry and a wet season to measure levels of land-based organic pollutants in this environment. Two types of passive sampling devices were deployed: (i) a polar sampler, which can be used to monitor polar herbicides and (ii) semipermeable membrane devices (SPMDs) which sequester more hydrophobic compounds (e.g. PAHs, chlorpyrifos). Herbicides (diuron, simazine, atrazine, hexazinone and/or flumeturon) were detected at low concentrations (ng L⁻¹) at all sites sampled and in both seasons. Chlorpyrifos was not detected while PAHs were present in SPMDs at levels below limits of detection. The results show that the GBR environment does contain low levels of organic pollutants and that passive sampling provides a sensitive monitoring tool for measuring waterborne organic pollutants.     

A Diffusive Sampler for Passive Monitoring of Underground Storage Tanks

Passive measurements of volatile organic compounds (VOCs) provide a method for early detection and long-term monitoring of potential leaks from underground storage tanks (USTs) and associated fuel service lines. A diffusive sampler was constructed of a sorbent tube that fits inside a specially designed sampling chamber. VOCs in the soil enter the chamber by molecular diffusion and are collected by the sorbent. The sorbent is easily retrieved for laboratory analyses by thermally desorbing into a gas chromatograph/mass spectrometer (GC/MS), or qualitative concentrations can be determined directly in the field with specific-indicator detectors.
The diffusive samplers were evaluated in an exposure chamber under controlled conditions. Laboratory measurements of the sorbed mass of organic vapor were found to be in close agreement with theoretical values and indicate the passive sampling approach is viable for detecting relatively low concentrations of organic vapors in the vadose zone over a one-day sampling period, as well as providing relatively long-term monitoring periods up to 58 days. A field test found the sampling approach successful in identifying an area where the vadose zone was contaminated by leaking petroleum USTs.     

Comparison of metal accumulation between 'Artificial Mussel' and natural mussels (Mytilus galloprovincialis) in marine environments

The passive sampler called 'Artificial Mussel' (AM) developed by Wu et al. (2007) can provide a time-integrated estimate of metal concentrations in the marine environment, and offers a potential device to assess and compare metal concentration in different marine environments worldwide. The aim of this study was to compare metal accumulation on AM and natural mussel Mytilus galloprovincialis at three sites with different metal loads along the Portuguese coast for four months. M. galloprovincialis were placed in cages alongside AMs at each site. Samples were collected monthly and Cd, Cr, Cu, Pb, and Zn concentrations in whole soft tissues and AMs compared. For both Cu and Cd, the results were similar between AMs and natural mussels. Higher concentrations of Zn were observed in natural mussels, whereas the inverse was shown for Pb (about 10-fold higher). Our results showed that AMs are promising tools for assessing metal concentrations in marine environments.     

Device for finely resolved sampling of littoral lake regions: Design and operation

Although littoral regions in northern lakes may sustain fish spawning grounds, little is known of the temporal or spatial aspects of their thermal and chemical regimes. This shortcoming is due in part to the difficulty in properly sampling these regions throughout the year with adequate spatial resolution. This problem is especially critical in lakes affected by episodic acidification during the spring snowmelt, a period of substantial importance to fisheries recruitment. A device was constructed to alleviate the problems associated with conventional water quality sampling of littoral regions. Constructed of thick walled polyvinyl chloride and permanently installed in the nearshore regions of an Adirondack lake, the episodic event sampler (EES) provided finely resolved (0.25 m) temperature and water chemistry data during the spring snowmelt period (February to May) of 1989. Although the construction and installation of the sampler represented a significant investment in labour and materials, this was offset by the high quality of the data collected. As the samplers were relatively undamaged by freeze-thaw activity, it is expected that they will continue to provide excellent information for several years.     

Comparison of Temporal Trends in VOCs as Measured with PDB Samplers and Low-Flow Sampling Methods

The effectiveness of passive diffusion bag (pdb) samplers in the measurement of selected volatile organic compounds (VOCs) is dependent on a number of factors. At some sites and wells, pdb sampling methods provide an attractive alternative to other sampling methods. In this discussion, I provide two examples of comparisons of temporal trends in tetrachloroethylene (PCE) concentrations from passive and low-flow sampling methods. At the example field site, large changes in PCE concentrations occurred over the deployment period(s) of the pdb samplers, yet the concentrations from the pdb samples are similar to the low-flow samples and the overall trends are the same.